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Chemical Structure| 67029-87-2 Chemical Structure| 67029-87-2

Structure of 67029-87-2

Chemical Structure| 67029-87-2

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Product Details of [ 67029-87-2 ]

CAS No. :67029-87-2
Formula : C16H14O4
M.W : 270.28
SMILES Code : O=C(C1=CC(OC)=CC=C1O)CC(C2=CC=CC=C2)=O
MDL No. :MFCD02043576

Safety of [ 67029-87-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 67029-87-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 67029-87-2 ]

[ 67029-87-2 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 67029-87-2 ]
  • [ 26964-24-9 ]
YieldReaction ConditionsOperation in experiment
94% With malic acid In neat (no solvent) at 140℃; for 0.166667 h; Green chemistry General procedure: The mixture of 1-(2-hydroxyphenyl)-3-aryl-1,3-propanedione 1a (0.5 g) and malic acid (1.0 eq.) was heatedeither in an oil bath, preheated at 140 °C for 10 min or in amicrowave reactor for 5 min. After the completion of reaction(TLC check), the reaction mixture was allowed to cool;at room temperature water (10 mL) and ethyl acetate (10mL) were added. Reaction mixture was neutralized by additionof solid NaHCO3. Organic layer was separated and theaqueous layer was extracted in ethyl acetate (2 10 mL).Combined organic extract was dried over anhydrous sodiumsulfate and concentrated in vacuo. The crude product waspurified by column chromatography on silica gel using hexane-ethylacetate solvent system to give the correspondingflavones in high yield.
91% With ammonium acetate In neat (no solvent) at 114℃; for 0.0833333 h; Microwave irradiation General procedure: The mixture of 1-(2-hydroxyphenyl)-3-aryl-1,3-propanedione 1a (0.5 g, 2.08 mmol) and ammonium acetate (0.16 g, 2.08 mmol) was heated either in an oil bath, preheated at 114°C for 10 min or in a microwave reactor for 5min. After the pH of the reaction mixture was brought back to 7.0 by the careful addition of NaHCO3 solution. The aqueous layer was extracted with ethyl acetate, dried(Na2SO4), and concentrated in vacuo. The crude product was purified by column chromatography on silica gel using hexane-ethyl acetate solvent system to give the corresponding flavones in high yield.
91% at 180℃; General procedure: The mixture of 1-(2-hydroxyphenyl)-3-aryl-1,3-propanedione 4a-q (0.5g, 2.08 mmol) and L-ascorbic acid(3.7g, 2.08 mmol) was heated on a preheated oil bath or undermicrowave irradiation at 180 °C for 2-3 min. After completionof reaction (TLC check), the reaction mixture wascooled to room temperature and the flask was sonicated byadding excess water. The crude product was filtered oversuction-pump and washed with excess of water to removeL-ascorbic acid. The solid obtained was dried and crystallizedby using ethanol to give the corresponding flavones inhigh yield. The purity of products was confirmed by satisfactoryspectroscopic data.
88% With zinc(II) oxide In neat (no solvent) at 100℃; for 0.25 h; Microwave irradiation; Green chemistry General procedure: A mixture of substituted 1,3-propanedione (0.5 g, 2.08 mmol, 1.0 eq.) and ZnO nanoparticles (1.0eq.) was heated in a microwave oven for 15 min. Same procedure used for purification of flavones as mentioned in the conventional heating method.
78% at 100℃; for 1 h; General procedure: Compounds 4a–j (1.8 g) glycerol triacetate (10 mL) and concentrated sulfuric acid (0.4 mL) wereplaced in a round bottomed flask equipped with a reflux condenser, stirred about 1 h at 100 C andthen the mixture was poured into a beaker containing 50 g of crushed ice, where solids were formedafter stirring and then filtered from the solution, Next the solids were washed with water until the acidwas removed. Finally, the solids were purified and separated by column chromatography eluting witha mixed petroleum ether and ethyl acetate solvent until the final products 5a–j were obtained. 6-Methoxyflavone (5a). Yield: 78percent; white solid, mp.: 163–165 °C; 1H-NMR (CDCl3) δ 7.93–7.80 (m,1H), 7.52 (t, J = 7.6 Hz, 2H), 7.51–7.39 (m, 1H), 7.24 (d, J = 3.1 Hz, 1H), 7.22 (d, J = 3.1 Hz, 2H), 7.19 (s,1H), 6.79 (s, 1H), 3.85 (s, 3H); 13C-NMR (CDCl3) δ 177.27, 162.12, 155.98, 150.04, 130.83, 130.46, 127.99,127.99, 125.20, 125.20, 123.52, 122.76, 118.48, 105.79, 103.81, 54.90. MS (ESI-MS) m/z calcd for C16H12O3[M + H]+: 253.26; found: 253.28.

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[2] Letters in Organic Chemistry, 2014, vol. 11, # 8, p. 601 - 605.
[3] Journal of Chemical Research, 2005, # 9, p. 556 - 557.
[4] Letters in Organic Chemistry, 2015, vol. 12, # 8, p. 574 - 583.
[5] Letters in Organic Chemistry, 2016, vol. 13, # 10, p. 734 - 741.
[6] Asian Journal of Chemistry, 2019, vol. 31, # 5, p. 1133 - 1136.
[7] Molecules, 2018, vol. 23, # 9, .
[8] Journal of Chemical Research - Part S, 1998, # 6, p. 348 - 349.
[9] Journal of the Chinese Chemical Society, 2004, vol. 51, # 6, p. 1389 - 1394.
[10] Journal of the Chemical Society, 1950, p. 1252,1257.
[11] Journal of Organic Chemistry, 1991, vol. 56, # 26, p. 7292 - 7297.
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